Fortrea is looking for a Clinical Data Scientist - R Programmer to join our team in Poland in a fully remote setup.

In this role, you will support Centralized Monitoring by configuring and maintaining systems, setting up new studies, and developing standard and bespoke monitoring functionalities. You will work closely with Data Scientists to ensure high-quality, efficient data oversight across clinical trials

Key Responsibilities

• Develop and maintain R programs to support RBQM (Risk based Quality Management) for clinical trial data 

• Collaborate with cross-functional teams to understand and implement project-specific data needs

• Provide technical expertise and support for data analysis and reporting tasks

• Perform quality control and validation of outputs to ensure accuracy and consistency

• Contribute to process improvements and development of programming standards using R

Qualifications

• Bachelor's degree in a quantitative field (e.g., Statistics, Mathematics, Computer Science, Data Science)

• Minimum of 2 years of experience in R programming including familiarity with R packages (e.g., Tidyverse, ggplot2, survival)

• Familiarity with data visualization techniques and tools in R

• Experience with clinical trial data

• Knowledge in Industry R packages like ADMIRAL and OAK

• Strong analytical and problem-solving skills

• Excellent communication and teamwork abilities

 Desirable Skills

• Knowledge of other open-source packages and tools

• Experience with SAS software

• Familiarity with CRAN, POSIT, and other open-source repositories and products

Learn more about our EEO & Accommodations request here.